ClinVar Miner

Variants in gene NCF2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
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NM_000433.3(NCF2):c.1081A>T (p.Thr361Ser) rs147744729
NM_000433.3(NCF2):c.113G>A (p.Arg38Gln) rs147415774
NM_000433.3(NCF2):c.1184G>A (p.Arg395Gln) rs145229115
NM_000433.3(NCF2):c.563G>A (p.Arg188Lys) rs115365142
NM_000433.4(NCF2):c.196C>A (p.Arg66=)
NM_000433.4(NCF2):c.197G>A (p.Arg66Gln) rs142803799
NM_000433.4(NCF2):c.938C>T (p.Pro313Leu) rs137937390

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